Canonical Allele Identifier: CA409630845

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63346758A>G , CM000682.2:g.63346758A>G	GRCh38
NC_000020.10:g.61978110A>G , CM000682.1:g.61978110A>G	GRCh37
NC_000020.9:g.61448554A>G	NCBI36
NG_011931.1:g.19586T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1864T>C MANE Select	ENSP00000359285.4:p.Trp622Arg
ENST00000370263.8:c.1864T>C	ENSP00000359285.4:p.Trp622Arg
ENST00000463705.5:n.2512T>C
ENST00000467563.3:n.1934T>C
ENST00000498043.6:c.1888T>C
ENST00000615287.4:c.1651T>C	ENSP00000483388.1:p.Trp551Arg
ENST00000627000.1:c.*1553T>C	ENSP00000486914.1:n.*1553T>C
ENST00000631289.1:n.178T>C
NM_000744.6:c.1864T>C	NP_000735.1:p.Trp622Arg
NM_001256573.1:c.1336T>C	NP_001243502.1:p.Trp446Arg
NR_046317.1:n.2120T>C
XM_011528524.1:c.1651T>C	XP_011526826.1:p.Trp551Arg
XM_017027625.2:c.1336T>C	XP_016883114.1:p.Trp446Arg
XM_024451822.1:c.1336T>C	XP_024307590.1:p.Trp446Arg
NM_001256573.2:c.1336T>C	NP_001243502.1:p.Trp446Arg
NR_046317.2:n.2073T>C
NM_000744.7:c.1864T>C MANE Select	NP_000735.1:p.Trp622Arg